Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10265937
rs10265937
SDK1
1 1.000 0.080 7 4034017 intron variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs10266101
rs10266101
SDK1
1 1.000 0.080 7 4034187 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10278187
rs10278187
SDK1
1 1.000 0.080 7 4034741 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1031458
rs1031458
GSDMB
1 1.000 0.080 17 39915920 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10445308
rs10445308
IKZF3
3 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10445371
rs10445371
MAPT
3 0.925 0.120 17 45988044 intron variant G/A snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs10485860
rs10485860
SDK1
1 1.000 0.080 7 4050651 intron variant T/C snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1077358
rs1077358
MANBA
1 1.000 0.080 4 102632769 intron variant C/T snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs1078268
rs1078268
MAPT ; STH
3 0.925 0.120 17 45998535 intron variant A/G snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs10852936
rs10852936
ZPBP2
2 0.925 0.120 17 39875461 intron variant C/T snv 0.39 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10889681
rs10889681
IL12RB2
1 0.925 0.160 1 67333487 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10931468
rs10931468
NAB1
1 0.925 0.080 2 190673836 intron variant C/A;G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs10982445
rs10982445
TNFSF8 ; DELEC1
1 1.000 0.080 9 114897411 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11078925
rs11078925
ZPBP2
3 0.925 0.160 17 39868955 intron variant T/C snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs11078929
rs11078929
PSMD3
1 1.000 0.080 17 39983981 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11191909
rs11191909
COL17A1
1 1.000 0.080 10 104053243 intron variant C/T snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs111972148
rs111972148
MAPT ; MAPT-AS1 ; MAPT-IT1
1 1.000 0.080 17 45895755 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11209050
rs11209050
IL12RB2
1 1.000 0.080 1 67326053 intron variant A/C snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs11209051
rs11209051
IL12RB2
1 1.000 0.080 1 67333212 intron variant C/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs11650661
rs11650661
ZPBP2
1 1.000 0.080 17 39870033 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11870965
rs11870965
ZPBP2
3 0.925 0.160 17 39873952 intron variant T/A snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs12150111
rs12150111
MAPT ; LOC105371800
2 1.000 0.080 17 45936572 intron variant A/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150127
rs12150127
KANSL1
1 1.000 0.080 17 46064366 intron variant G/A snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12150447
rs12150447
KANSL1
2 1.000 0.080 17 46050759 intron variant A/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs12155314
rs12155314
SDK1
1 1.000 0.080 7 4041562 intron variant G/T snv 0.24 0.700 1.000 1 2012 2012